EA200101268A1 - Способ тиазола, фармацевтические препараты для ингибирования протеинкиназ и способы их применения - Google Patents

Способ тиазола, фармацевтические препараты для ингибирования протеинкиназ и способы их применения

Info

Publication number
EA200101268A1
EA200101268A1 EA200101268A EA200101268A EA200101268A1 EA 200101268 A1 EA200101268 A1 EA 200101268A1 EA 200101268 A EA200101268 A EA 200101268A EA 200101268 A EA200101268 A EA 200101268A EA 200101268 A1 EA200101268 A1 EA 200101268A1
Authority
EA
Eurasian Patent Office
Prior art keywords
compounds
modulate
cell proliferation
pharmaceutical preparations
preparations containing
Prior art date
Application number
EA200101268A
Other languages
English (en)
Russian (ru)
Inventor
Сяо Сонг Чу
Ларри Эндрю Алегрия
Стивен Ли Бендер
Сюзанн Притчет Бенедикт
Аллен Дж. Борчардт
Роберт Стивен Кания
Митчелл Дэвид Намбу
Анна Мария Темпчик-Расселл
Сепер Саршар
Дилип Бхумралкар
Женгвей Пенг
Йи Мишель Янг
Original Assignee
Агурон Фармасьютикалз, Инк.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Агурон Фармасьютикалз, Инк. filed Critical Агурон Фармасьютикалз, Инк.
Publication of EA200101268A1 publication Critical patent/EA200101268A1/ru

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D277/38Nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/60Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D277/62Benzothiazoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6536Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and sulfur atoms with or without oxygen atoms, as the only ring hetero atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6536Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and sulfur atoms with or without oxygen atoms, as the only ring hetero atoms
    • C07F9/6539Five-membered rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6558Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
    • C07F9/65583Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
EA200101268A 1999-06-04 2000-06-02 Способ тиазола, фармацевтические препараты для ингибирования протеинкиназ и способы их применения EA200101268A1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US13781099P 1999-06-04 1999-06-04
PCT/US2000/015188 WO2000075120A1 (fr) 1999-06-04 2000-06-02 Diaminothiazoles et leur utilisation pour inhiber les proteines kinases

Publications (1)

Publication Number Publication Date
EA200101268A1 true EA200101268A1 (ru) 2002-06-27

Family

ID=22479135

Family Applications (1)

Application Number Title Priority Date Filing Date
EA200101268A EA200101268A1 (ru) 1999-06-04 2000-06-02 Способ тиазола, фармацевтические препараты для ингибирования протеинкиназ и способы их применения

Country Status (34)

Country Link
US (1) US6620828B2 (fr)
EP (1) EP1181283B1 (fr)
JP (1) JP2003501420A (fr)
KR (1) KR20020015333A (fr)
CN (1) CN1359380A (fr)
AP (1) AP2001002341A0 (fr)
AT (1) ATE288424T1 (fr)
AU (1) AU778071B2 (fr)
BG (1) BG106276A (fr)
BR (1) BR0011585A (fr)
CA (1) CA2371158A1 (fr)
CZ (1) CZ20014213A3 (fr)
DE (1) DE60017894T2 (fr)
EA (1) EA200101268A1 (fr)
EE (1) EE200100659A (fr)
ES (1) ES2234628T3 (fr)
HR (1) HRP20020008A2 (fr)
HU (1) HUP0202897A3 (fr)
IL (1) IL146094A0 (fr)
IS (1) IS6183A (fr)
MA (1) MA25530A1 (fr)
MX (1) MXPA01012483A (fr)
NO (1) NO20015045L (fr)
NZ (1) NZ514881A (fr)
OA (1) OA11959A (fr)
PE (1) PE20010211A1 (fr)
PL (1) PL352714A1 (fr)
SK (1) SK17302001A3 (fr)
SV (1) SV2002000096A (fr)
UA (1) UA71971C2 (fr)
UY (1) UY26190A1 (fr)
WO (1) WO2000075120A1 (fr)
YU (1) YU85601A (fr)
ZA (1) ZA200108291B (fr)

Families Citing this family (63)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020150921A1 (en) * 1996-02-09 2002-10-17 Francis Barany Detection of nucleic acid sequence differences using the ligase detection reaction with addressable arrays
CA2306082A1 (fr) * 1997-10-27 1999-05-06 Agouron Pharmaceuticals, Inc. Composes de 4-amino-thiazol-2-y substitues comme inhibiteurs cdks
US6262096B1 (en) 1997-11-12 2001-07-17 Bristol-Myers Squibb Company Aminothiazole inhibitors of cyclin dependent kinases
US20040226056A1 (en) * 1998-12-22 2004-11-11 Myriad Genetics, Incorporated Compositions and methods for treating neurological disorders and diseases
US7125875B2 (en) 1999-04-15 2006-10-24 Bristol-Myers Squibb Company Cyclic protein tyrosine kinase inhibitors
ES2391550T3 (es) 1999-04-15 2012-11-27 Bristol-Myers Squibb Company Inhibidores cíclicos de la proteína tirosina quinasa
EP1347971B1 (fr) 2000-12-21 2006-03-01 Bristol-Myers Squibb Company Inhibiteurs thiazolyl des tyrosine kinases de la famille tec
US6756374B2 (en) 2001-01-22 2004-06-29 Hoffmann-La Roche Inc. Diaminothiazoles having antiproliferative activity
UA76977C2 (en) 2001-03-02 2006-10-16 Icos Corp Aryl- and heteroaryl substituted chk1 inhibitors and their use as radiosensitizers and chemosensitizers
MXPA03011196A (es) * 2001-06-08 2004-10-28 Cytovia Inc 3-aril-5-aril-[1,2,4]-oxadiazoles sustituidos y analogos.
CA2474322A1 (fr) * 2002-01-25 2003-07-31 Kylix Pharmaceuticals B.V. (thia-/oxa-/pyra) zoles substitues 4(hetero-) aryle pour inhibition de tie-2
US6818663B2 (en) * 2002-05-17 2004-11-16 Hoffmann-La Roches Diaminothiazoles
ATE375342T1 (de) 2002-08-02 2007-10-15 Ab Science 2-(3-aminoaryl)amino-4-aryl-thiazole und ihre verwendung als c-kit inhibitoren
US8450302B2 (en) 2002-08-02 2013-05-28 Ab Science 2-(3-aminoaryl) amino-4-aryl-thiazoles and their use as c-kit inhibitors
TW200416029A (en) * 2002-11-01 2004-09-01 Takeda Chemical Industries Ltd Agent for preventing or treating neuropathy
WO2004074283A1 (fr) * 2003-02-21 2004-09-02 Pfizer Inc. Derives d'amino-thiazole substitues par n-heterocyclyle en tant qu'inhibiteurs de la proteine kinase
US7078419B2 (en) 2003-03-10 2006-07-18 Boehringer Ingelheim Pharmaceuticals, Inc. Cytokine inhibitors
SI3889142T1 (sl) 2003-04-11 2022-10-28 Ptc Therapeutics, Inc. Spojine 1,2,4-oksadiazol benzojske kisline in njihova uporaba za zatiranje nesmiselne ter zdravljenje bolezni
WO2004092217A1 (fr) * 2003-04-17 2004-10-28 Pfizer Inc. Structure cristalline de complexes du domaine kinase du recepteur du facteur de croissance endothelial vasculaire (vegfrkd) et de ligands et leurs procedes d'utilisation
EP1644323B1 (fr) * 2003-07-07 2015-03-18 Georgetown University Inhibiteurs d'histone desacetylase et leurs procedes d'utilisation
CA2536954C (fr) 2003-08-29 2012-11-27 Exelixis, Inc. Modulateurs c-kit et leurs procedes d'utilisation
WO2005037235A2 (fr) * 2003-10-16 2005-04-28 Imclone Systems Incorporated Inhibiteurs du recepteur 1 du facteur de croissance du fibroblaste et methodes therapeutiques associees
EP1709019B1 (fr) * 2004-01-12 2007-08-08 Applied Research Systems ARS Holding N.V. Dérivés de thiatole et leur utilisation
WO2005108370A1 (fr) * 2004-04-16 2005-11-17 Ajinomoto Co., Inc. Composés du benzène
US7211576B2 (en) 2004-04-20 2007-05-01 Hoffmann-La Roche Inc. Diaminothiazoles
CA2573413C (fr) * 2004-07-12 2010-02-09 Merck & Co., Inc. Inhibiteurs de l'histone desacetylase
AU2006251157B2 (en) 2005-05-24 2011-09-01 Merck Serono Sa Thiazole derivatives and use thereof
JP5290751B2 (ja) * 2005-05-24 2013-09-18 メルク セローノ ソシエテ アノニム チアゾール誘導体及びそれらの使用
SI2395002T1 (sl) 2005-11-08 2014-10-30 Vertex Pharmaceuticals Incorporated Farmacevtski sestavek, vsebujoč heterociklični modulator prenašalcev z ATP-vezavno kaseto
AU2012244242B2 (en) * 2005-12-28 2015-05-21 Vertex Pharmaceuticals Incorporated 1-(benzo [D] [1,3] dioxol-5-yl) -N- (phenyl) cyclopropane- carboxamide derivatives and related compounds as modulators of ATP-Binding Cassette transporters for the treatment of Cystic Fibrosis
CA2635760C (fr) * 2005-12-28 2014-07-15 Vertex Pharmaceuticals Incorporated Modulateurs de transporteurs a cassette liant l'atp
BRPI0706621A2 (pt) * 2006-01-18 2011-04-05 Amgen Inc composto, composição farmacêutica, métodos para tratar um distúrbio mediado por quinase em um mamìfero e para tratar um distúrbio relacionado com a proliferação em um mamìfero, e , uso do composto
CN101384568B (zh) * 2006-02-15 2012-12-12 雅培制药有限公司 乙酰辅酶a羧化酶(acc)抑制剂及其在糖尿病、肥胖症和代谢综合征中的应用
US8748627B2 (en) * 2006-02-15 2014-06-10 Abbvie Inc. Acetyl-CoA carboxylase (ACC) inhibitors and their use in diabetes, obesity and metabolic syndrome
SG170819A1 (en) 2006-03-30 2011-05-30 Ptc Therapeutics Inc Methods for the production of functional protein from dna having a nonsense mutation and the treatment of disorders associated therewith
WO2008003770A1 (fr) 2006-07-07 2008-01-10 Boehringer Ingelheim International Gmbh Dérivés d'hétéroaryle substitués par phényle et leur utilisation en tant qu'agents antitumoraux
US7879856B2 (en) 2006-12-22 2011-02-01 Rigel Pharmaceuticals, Inc. Diaminothiazoles useful as Axl inhibitors
JP5497633B2 (ja) 2007-05-09 2014-05-21 バーテックス ファーマシューティカルズ インコーポレイテッド Cftrのモジュレーター
JP2010531850A (ja) * 2007-07-02 2010-09-30 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 新規化合物
CL2008001943A1 (es) 2007-07-02 2009-09-11 Boehringer Ingelheim Int Compuestos derivados de fenil-triazol, inhibidores de enzimas de señales especificas que participan del control de la proliferacion celular; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar cancer, infecciones, enfermedades inflamatorias y autoinmunes.
CA2692713A1 (fr) 2007-07-17 2009-01-22 Amgen Inc. Modulateurs heterocycliques de pkb
WO2009011871A2 (fr) * 2007-07-17 2009-01-22 Amgen Inc. Thiadiazoles modulateurs de l'activité de pkb
AU2008335440B2 (en) 2007-12-07 2013-11-07 Vertex Pharmaceuticals Incorporated Processes for producing cycloalkylcarboxamido-pyridine benzoic acids
WO2009073757A1 (fr) 2007-12-07 2009-06-11 Vertex Pharmaceuticals Incorporated Formes solides d'acide 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)-3-méthylpyridin-2-yl)benzoïque
JP2011506454A (ja) * 2007-12-13 2011-03-03 グラクソスミスクライン エルエルシー チアゾールおよびオキサゾールキナーゼ阻害薬
US8299099B2 (en) 2008-02-28 2012-10-30 Vertex Pharmaceuticals Incorporated Heteroaryl derivatives as CFTR modulators
UA103319C2 (en) 2008-05-06 2013-10-10 Глаксосмитклайн Ллк Thiazole- and oxazole-benzene sulfonamide compounds
US8778929B2 (en) 2008-09-29 2014-07-15 Boehringer Ingelheim International Gmbh Substituted heteroaryl inhibitors of B-RAF
CN102281875B (zh) 2009-01-16 2017-09-22 里格尔药品股份有限公司 预防、治疗或应对转移癌的使用axl抑制剂的组合疗法
EP2492269A4 (fr) * 2009-10-19 2013-08-07 Taisho Pharmaceutical Co Ltd Dérivé de l'aminothiazole
EP2552907B1 (fr) 2010-03-26 2014-10-22 Boehringer Ingelheim International GmbH Pyridyltriazoles
WO2011117381A1 (fr) 2010-03-26 2011-09-29 Boehringer Ingelheim International Gmbh Inhibiteurs de kinase b-raf
WO2011127241A2 (fr) 2010-04-07 2011-10-13 Vertex Pharmaceuticals Incorporated Compositions pharmaceutiques de l'acide 3-(6-(1-(2,2-difluorobenzo [d] [1,3] dioxol-5-yle) cyclopropane carboxamido)-3-méthylpyridin-2-yle) benzoïque et leur administration
US8710055B2 (en) 2010-12-21 2014-04-29 Boehringer Ingelheim International Gmbh Triazolylphenyl sulfonamides as serine/threonine kinase inhibitors
WO2013161919A1 (fr) * 2012-04-26 2013-10-31 小野薬品工業株式会社 COMPOSÉ INHIBITEUR DE Trk
BR112015019921A2 (pt) 2013-02-19 2017-07-18 Ono Pharmaceutical Co composto inibidor de trk
GB201309333D0 (en) * 2013-05-23 2013-07-10 Agency Science Tech & Res Purine diones as WNT pathway modulators
WO2015073231A1 (fr) 2013-11-12 2015-05-21 Vertex Pharmaceuticals Incorporated Procédé de préparation de compositions pharmaceutiques pour le traitement de maladies à médiation assurée par le cftr
US9873677B2 (en) 2014-03-06 2018-01-23 Ptc Therapeutics, Inc. Pharmaceutical compositions and salts of a 1,2,4-oxadiazole benzoic acid
WO2016081556A1 (fr) 2014-11-18 2016-05-26 Vertex Pharmaceuticals Incorporated Procédé pour effectuer une chromatographie liquide haute performance pour un test à haut rendement
CN108348527A (zh) 2015-10-30 2018-07-31 Ptc医疗公司 用于治疗癫痫的方法
CA3036245C (fr) * 2016-09-13 2021-07-20 Arbutus Biopharma Corporation Composes de chromane-8-carboxamide substitues et analogues de ceux-ci, et procedes les utilisant
CN111233786B (zh) * 2020-02-04 2021-11-26 中国人民解放军军事科学院军事医学研究院 含五元杂环的苯磺酰胺类化合物及其制备方法和用途

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE273062C (de) 1912-04-19 1914-04-20 Deylen Sohn Firma Vorrichtung zum Schränken von Plattenzündspänen
AU558132B2 (en) 1981-05-27 1987-01-22 Labatt Brewing Co. Ltd. Malt sterilisation with hydrogen peroxide
US4994479A (en) 1985-04-03 1991-02-19 Yamanouchi Pharmaceutical Co., Ltd. Phenylene derivatives and anti-allergic use thereof
US5409930A (en) * 1991-05-10 1995-04-25 Rhone-Poulenc Rorer Pharmaceuticals Inc. Bis mono- and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase
CA2130196A1 (fr) 1992-03-24 1993-09-30 Jose Luis Castro Pineiro Derives de la benzodiazepine
US5631156A (en) 1994-06-21 1997-05-20 The University Of Michigan DNA encoding and 18 KD CDK6 inhibiting protein
WO1996014843A2 (fr) 1994-11-10 1996-05-23 Cor Therapeutics, Inc. Compositions pharmaceutiques a base de pyrazole, agissant comme inhibiteurs des proteines kinases
ATE197300T1 (de) 1995-02-02 2000-11-15 Smithkline Beecham Plc Indolderivate als 5-ht rezeptorantagoniste
US5710173A (en) 1995-06-07 1998-01-20 Sugen, Inc. Thienyl compounds for inhibition of cell proliferative disorders
WO1997003967A1 (fr) 1995-07-22 1997-02-06 Rhone-Poulenc Rorer Limited Composes aromatiques substitues et leur utilisation pharmaceutique
US5705499A (en) 1995-10-06 1998-01-06 Boehringer Ingelheim Pharmaceuticals, Inc. 8-arylalkyl- and 8-arylheteroalkyl-5,11-dihydro-6H-dipyrido 3,2-B:2',3'-e! 1!diazepines and their use in the treatment of HIV-1 infection
US5733920A (en) 1995-10-31 1998-03-31 Mitotix, Inc. Inhibitors of cyclin dependent kinases
US5760028A (en) 1995-12-22 1998-06-02 The Dupont Merck Pharmaceutical Company Integrin receptor antagonists
DE69734149T2 (de) 1996-03-15 2006-07-06 Astrazeneca Ab Cinoline derivate und verwendung als heilmittel
ATE211740T1 (de) 1996-06-27 2002-01-15 Pfizer Substituierte indazolderivate
IL128642A0 (en) 1996-09-04 2000-01-31 Pfizer Indazole derivatives and their use as inhibitors of phosphodiesterase (pde) type iv and the production of tumor necrosis factor (tnf)
ID18494A (id) 1996-10-02 1998-04-16 Novartis Ag Turunan pirazola leburan dan proses pembuatannya
CA2306082A1 (fr) * 1997-10-27 1999-05-06 Agouron Pharmaceuticals, Inc. Composes de 4-amino-thiazol-2-y substitues comme inhibiteurs cdks
SK6252000A3 (en) 1997-11-04 2001-11-06 Pfizer Prod Inc Indazole bioisostere replacement of catechol in therapeutically active compounds
HUP0100330A3 (en) 1997-11-04 2002-03-28 Pfizer Prod Inc Therapeutically active compounds based on indazole bioisostere replacement of catechol in pde4 inhibitors, compositions containing them and their use
US6040321A (en) * 1997-11-12 2000-03-21 Bristol-Myers Squibb Company Aminothiazole inhibitors of cyclin dependent kinases
ES2237919T4 (es) * 1998-06-18 2007-05-01 Bristol-Myers Squibb Company Inhibidores aminotiazol sustituidos con carbono de quinasas dependientes de ciclina.
PT1117659E (pt) 1998-09-29 2004-04-30 Wyeth Corp Cianoquinolinas substituidas como inibidores de tirosina-quinases de proteinas

Also Published As

Publication number Publication date
KR20020015333A (ko) 2002-02-27
EP1181283B1 (fr) 2005-02-02
IS6183A (is) 2001-11-29
UA71971C2 (en) 2005-01-17
NZ514881A (en) 2003-10-31
CN1359380A (zh) 2002-07-17
HRP20020008A2 (en) 2004-02-29
AP2001002341A0 (en) 2001-12-31
DE60017894D1 (de) 2005-03-10
ES2234628T3 (es) 2005-07-01
EP1181283A1 (fr) 2002-02-27
SK17302001A3 (sk) 2004-01-08
MXPA01012483A (es) 2002-07-30
UY26190A1 (es) 2000-12-29
WO2000075120A1 (fr) 2000-12-14
AU5725400A (en) 2000-12-28
OA11959A (en) 2006-04-17
IL146094A0 (en) 2002-07-25
CZ20014213A3 (cs) 2002-04-17
YU85601A (sh) 2004-09-03
US6620828B2 (en) 2003-09-16
AU778071B2 (en) 2004-11-11
MA25530A1 (fr) 2002-10-01
JP2003501420A (ja) 2003-01-14
HUP0202897A2 (hu) 2002-12-28
CA2371158A1 (fr) 2000-12-14
DE60017894T2 (de) 2005-12-29
ATE288424T1 (de) 2005-02-15
HUP0202897A3 (en) 2004-12-28
BR0011585A (pt) 2002-03-19
PE20010211A1 (es) 2001-03-16
PL352714A1 (en) 2003-09-08
US20020025976A1 (en) 2002-02-28
NO20015045D0 (no) 2001-10-17
EE200100659A (et) 2003-02-17
NO20015045L (no) 2002-02-04
ZA200108291B (en) 2002-12-24
SV2002000096A (es) 2002-06-07
BG106276A (bg) 2002-10-31

Similar Documents

Publication Publication Date Title
EA200101268A1 (ru) Способ тиазола, фармацевтические препараты для ингибирования протеинкиназ и способы их применения
EA200200120A1 (ru) Соединения индазола, фармацевтические препараты для ингибирования протеинкиназ и способы их применения
TWI262914B (en) Compounds and pharmaceutical compositions for inhibiting protein kinases
EA200200768A1 (ru) Соединения индазола, фармацевтические композиции и методы модуляции или ингибирования клеточной пролиферации
EA199900021A1 (ru) Бициклические гетероароматические соединения в качестве ингибиторов протеинтирозинкиназы
EA200500811A1 (ru) 2-(1h-индазол-6-иламино)бензамидные соединения как ингибиторы протеинкиназ, полезные для лечения офтальмологических заболеваний
MXPA06001193A (es) Compuestos de indazol 3,5-disustituidos, composiciones farmaceuticas y metodos para intervenir en o inhibir la proliferacion celular.
BR0108025A (pt) Compostos de amida, sal farmaceuticamente aceitável de um metabólito farmaceuticamente ativo do composto, composição farmacêutica para modular ou inibir a atividade de um receptor de proteìna cinase, método de tratamento de uma condição doentia de mamìferos mediada pela atividade de proteìna cinase e método para modular ou inibir a atividade de um receptor de proteìna cinase
EA199900022A1 (ru) Бициклические гетероароматические соединения в качестве ингибиторов протеинтирозинкиназы
DE69738949D1 (de) Chinolincarboxamide als tnf-inhibitoren und als pde-iv inhibitoren
ATE265456T1 (de) 2-amino-6-anilino-purine und deren verwendung als arzneimittel
EA200200473A1 (ru) Ингибиторы тирозинкиназы
ATE354372T1 (de) Verwendung von mif-antagonisten zur krebstherapie
DE69426334T2 (de) Parenterales Busulfan zur Behandlung von malignen Krankheiten
HUP0002427A2 (hu) Leptin mint tumorsejt proliferációt gátló hatóanyag és alkalmazása
FR2736915B1 (fr) Variants de la proteine p53 et utilisations therapeutiques
MXPA03001189A (es) Compuestos de pirazol-tiazol, composiciones farmaceuticas que los contienen y su uso para inhibir las cinasas dependientes de ciclinas.
MXPA03001452A (es) Hidroximino-fluorenos heterociclicos y su uso para la inhibicion de las proteinas cinasas.
DE69814691D1 (de) Verwendung von fc101 als hemmstoff der angiogenese zur behandlung von krebs und anderen angiogenen krankheiten
TH75180B (th) สารประกอบอินดาโซลและองค์ประกอบทางเภสัชภัณฑ์ในการยับยั้งโปรตีนไคเนสและวิธีใช้ประโยชน์
BR0109570A (pt) Compostos compreendendo uma parte especìfica de célula alvo e uma parte citotóxica, e uma parte mediadora capaz de reconhecer uma molécula especìfica de célula alvo e uma segunda parte citotóxica, molécula de ácido nucleico isolada, método para fabricar um composto, vetor para expressar em uma célula hospedeira, um composto, ou uma parte deste, célula hospedeira, composição farmacêutica, uso de um composto, e método para tratar um paciente tendo células alvo a serem destruìdas
TH140338A (th) สารประกอบอินดาโซลและองค์ประกอบทางเภสัชภัณฑ์ในการยับยั้งโปรตีนไคเนสและวิธีใช้ประโยชน์
UY26547A1 (es) Compuestos de amida y composiciones farmacéuticas para inhibir proteinquinasas, y su modo de empleo